By Rachel Hull, Biochemistry and Molecular Biology, ’19
“I decided to write this piece after stumbling across several news articles in October of this year heralding the birth of the first ever ‘three-parent baby’ and thinking to myself that something seemed to be missing in these stories. What started as some casual digging into the history of three-parent babies soon turned into a more general investigation of assisted reproductive technologies. The information I found was not only interesting but also very pertinent, as new advances could increase the role these technologies play in our society.“
Continue reading A Glimpse into Mitochondrial Replacement Techniques
By Lo Tuan, Neurobiology, Physiology, and Behavior and Managerial Economics, ’17
“I chose to write about Tourette Syndrome because someone who is dear to me was diagnosed with it. Watching him struggle at a young age, I could only imagine how difficult it must have been dealing with strange and disapproving looks from peers and teachers. Through the gradual decline of symptoms over the years, he learned to cope with his tics and sought to educate others about the syndrome. Inspired by his story, I wrote this case report in hopes of share his journey with others.”
Continue reading A Case Report of Tourette Syndrome
By: Esther Ebuehi, Human Development major, Nutrition Science minor ’16
“This narrative case report describes an athlete’s shoulder injury and explores the way injuries are treated in the world of collegiate athletics. While I was writing this piece, I recognized just how little time non-athletes spend thinking about the impact of sports injuries. Many NCAA athletes have life-long sports injuries, but we rarely talk about this issue as a campus community. There’s a national discourse revolving around injury prevention in football, and I believe this is a topic college students (athletes and non-athletes alike) should be thinking critically about.”
Continue reading The Fragile Physiology of Football Players
By David Ivanov, Biochemistry and Molecular Biology, 2015
Sjogren’s syndrome, like other autoimmune diseases, can be difficult to diagnose definitively, and often relies on a handful of signs and symptoms that can vary substantially from case to case. The only signs considered markers for Sjogren’s are anti-SSA and anti-SSB antibodies, and while anti-SSB is more specific, elevated levels of anti-SSB are actually less common in patients with Sjogren’s syndrome than anti-SSA, leading to some ambiguity in diagnosis.
A seventeen year old female patient presented with a large, soft, sublingual cyst on the left side of the floor of her mouth. While she reported no pain, the cyst was first spotted about a year earlier, and had been growing steadily. Visible swelling was observed on the left side of her face under her jaw line. Surgery was performed to remove the cyst, and an adjacent salivary gland was removed as well. The otorhinolaryngologist took a tissue sample, and histology confirmed a benign growth. The surgeon ordered a blood panel to evaluate antibody levels that might indicate an autoimmune disease. The patient’s serum was negative for rheumatoid factor, anti-SSB antibodies, and anti-nuclear antibodies. However, she was positive for anti-SSA antibodies, with a level of 50 U/ml. Bacterial cultures were negative for oral infection, and an X-ray was negative for sarcoidosis. Patient was discharged after surgery with no medications indicated, as she was not experiencing any other symptoms.
Continue reading Case Report: Sjogren’s Syndrome